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PMID: 17445271 已发表 · epublish 英语

Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescents.

BMC medical genetics ·第 8 卷 ·2007-05-09

Hölter Katja, Wermter Anne-Kathrin, Scherag André, Siegfried Wolfgang, Goldschmidt Hanspeter, Hebebrand Johannes, Hinney Anke

摘要

The suppressor of cytokine signaling (SOCS)-3 is a negative feedback regulator of cytokine signaling and also influences leptin signaling. We investigated association of variations in the coding sequence and promoter region of SOCS3 with extreme obesity in German children and adolescents.,An initial screen for sequence variations in 181 extremely obese children and adolescents and 188 healthy underweight adults revealed two previously reported single nucleotide polymorphisms (SNPs) in the SOCS3 5' region: -1044 C>A (numbering refers to bases upstream of ATG in exon 2) within a predicted STAT3 binding element and -920 C>A (rs12953258, for numbering, see above).,We did not detect significant differences in allele or genotype frequencies for any of these SNPs between the analysed study groups (all nominal p > 0.2). In addition, we performed a pedigree transmission disequilibrium test (PDT) for the SNP -1044 C>A in families comprising 703 obese children and adolescents, 281 of their obese siblings and both biological parents. The PDT revealed no transmission disequilibrium (nominal p > 0.05).,In conclusion, our data do not suggest evidence for a major role of the respective SNPs in SOCS3 in the pathogenesis of extreme obesity in our study groups.

文献信息
期刊
BMC medical genetics
期刊简称
BMC Med Genet
发表日期
2007-05-09
收录日期
2007-05-09
更新日期
2016-11-24
语言
英语
国家/地区
England
NLM ID
100968552
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